Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

DU 2550-E — Class IIb MDR by Philips Medical Systems…

MD Atlas
Philips Medical Systems DMC GmbH

EUDAMED last updated this device on Apr 17, 2025

DU 2550-E

0884838BM495TK

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Philips Medical Systems DMC GmbH
UDI-DI code: 00884838076488
Reference / catalog number: 989000086681

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Philips Medical Systems DMC GmbH
SRN: DE-MF-000005362
Manufacturer status: Active

Related devices

Mobile Detector Holder0884838BM448TAOn the market Adjustable Straps0884838BM447T8On the market Adult Headrest0884838BM447T8On the market Adult Headrest0884838BM447T8On the market Ankle Clamps0884838BM447T8On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	May 28, 2020	Dec 31, 9999

Device identification

Trade name: DU 2550-E
UDI-DI code: 00884838076488
Basic UDI-DI: 0884838BM495TK
Reference / catalog number: 989000086681
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: x-ray tube
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11039012X-RAY TUBE ASSEMBLY

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification